Evidence map›Paper›PMID 34572738›Full record

ArticleCancers2021

Nivolumab Reduces PD1 Expression and Alters Density and Proliferation of Tumor Infiltrating Immune Cells in a Tissue Slice Culture Model of Renal Cell Carcinoma.

Philipp J Stenzel, Nina Hörner, Sebastian Foersch, Daniel-Christoph Wagner, Igor Tsaur, Anita Thomas, Axel Haferkamp, Stephan Macher-Goeppinger, Wilfried Roth, Stefan Porubsky and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  3. Tumor-infiltrating plasma cells are a prognostic factor in penile squamous cell carcinoma.Virchows Archiv : an international journal of pathology · 2025
    Article
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  5. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Philipp J StenzelInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.ORCID 0000-0001-8153-5450
Nina HörnerInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.
Sebastian FoerschInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.
Daniel-Christoph WagnerInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.
Igor TsaurDepartment of Urology, University Medical Center Mainz, 55131 Mainz, Germany.ORCID 0000-0001-5107-3523
Anita ThomasDepartment of Urology, University Medical Center Mainz, 55131 Mainz, Germany.
Axel HaferkampDepartment of Urology, University Medical Center Mainz, 55131 Mainz, Germany.
Stephan Macher-GoeppingerInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.
Wilfried RothInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.
Stefan PorubskyInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.ORCID 0000-0002-7647-7265
Katrin E TagschererInstitute of Pathology, University Medical Center Mainz, 55131 Mainz, Germany.ORCID 0000-0002-0657-6399
Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the treatment of clear cell renal cell carcinoma (ccRCC), nivolumab is an established component of the first-line therapy with a favorable impact on progression free survival and overall survival. However, treatment-related adverse effects occur and, to date, there is no approved predictive biomarker for patient stratification. Thus, the aim of this study was to establish an ex vivo tissue slice culture model of ccRCC and to elucidate the impact of nivolumab on tumor infiltrating immune cells.

methodsFresh tumor tissue of ccRCC was treated with the immune checkpoint inhibitor nivolumab using ex vivo tissue slice culture (TSC). After cultivation, tissue slices were formalin-fixed, immunohistochemically stained and analyzed via digital image analysis.

resultsThe TSC model was shown to be suitable for ex vivo pharmacological experiments on intratumoral immune cells in ccRCC. PD1 expression on tumor infiltrating immune cells was dose-dependently reduced after nivolumab treatment (

conclusionsThis study could demonstrate nivolumab-dependent effects on PD1 expression and tumor infiltrating T-cells in TSC of ccRCC. This is in line with results from other scientific studies about changes in immune cell proliferation in peripheral blood in response to nivolumab. Thus, TSC of ccRCC could be a further step to personalized medicine in terms of testing the response of individual patients to nivolumab.

Indexed as

clear cell renal cell carcinomanivolumabPD1T-cellstissue slice culture

Identifiers

PMID34572738
PMCPMC8471479
OpenAlexW3196654051

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.